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S Lyonnet

Showing results (161-170 of 223) with videos related to

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Journal of Vascular Research|April 16, 2005
Vascular wall remodeling in patients with supravalvular aortic stenosis and Williams Beuren syndromeS M Dridi, A Foucault Bertaud, S Igondjo Tchen, et al.
Nature Genetics|November 1, 1996
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung diseaseR Salomon, T Attié, A Pelet, et al.
American Journal of Medical Genetics|July 23, 1998
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2V Cormier-Daire, A Superti-Furga, A Munnich, et al.
Journal of Medical Genetics|July 5, 2005
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)P J Ferguson, S Chen, M K Tayeh, et al.
American Journal of Medical Genetics|October 12, 2002
Clinical and genetic heterogeneity of Seckel syndromeL Faivre, M Le Merrer, S Lyonnet, et al.
Journal of Medical Genetics|January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locusL de Pontual, A Pelet, D Trochet, et al.
Human Molecular Genetics|December 1, 1994
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogeneL M Mulligan, C Eng, T Attié, et al.
American Journal of Medical Genetics|October 26, 1999
Skin elastic fibers in Williams syndromeS M Dridi, S Ghomrasseni, D Bonnet, et al.
Journal of Medical Genetics|March 2, 1999
A new lethal syndrome of exomphalos, short limbs, and macrogonadismL Faivre, A L Delezoide, F Narcy, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Pageof 23

Showing results (161-170 of 223) with videos related to

Sort By:
Pageof 23
Journal of Vascular Research|April 16, 2005
Vascular wall remodeling in patients with supravalvular aortic stenosis and Williams Beuren syndromeS M Dridi, A Foucault Bertaud, S Igondjo Tchen, et al.
Nature Genetics|November 1, 1996
Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung diseaseR Salomon, T Attié, A Pelet, et al.
American Journal of Medical Genetics|July 23, 1998
Clinical homogeneity of the Stüve-Wiedemann syndrome and overlap with the Schwartz-Jampel syndrome type 2V Cormier-Daire, A Superti-Furga, A Munnich, et al.
Journal of Medical Genetics|July 5, 2005
Homozygous mutations in LPIN2 are responsible for the syndrome of chronic recurrent multifocal osteomyelitis and congenital dyserythropoietic anaemia (Majeed syndrome)P J Ferguson, S Chen, M K Tayeh, et al.
American Journal of Medical Genetics|October 12, 2002
Clinical and genetic heterogeneity of Seckel syndromeL Faivre, M Le Merrer, S Lyonnet, et al.
Journal of Medical Genetics|January 31, 2006
Mutations of the RET gene in isolated and syndromic Hirschsprung's disease in human disclose major and modifier alleles at a single locusL de Pontual, A Pelet, D Trochet, et al.
Human Molecular Genetics|December 1, 1994
Diverse phenotypes associated with exon 10 mutations of the RET proto-oncogeneL M Mulligan, C Eng, T Attié, et al.
American Journal of Medical Genetics|October 26, 1999
Skin elastic fibers in Williams syndromeS M Dridi, S Ghomrasseni, D Bonnet, et al.
Journal of Medical Genetics|March 2, 1999
A new lethal syndrome of exomphalos, short limbs, and macrogonadismL Faivre, A L Delezoide, F Narcy, et al.
Journal of Medical Genetics|January 8, 2009
19q13.11 deletion syndrome: a novel clinically recognisable genetic condition identified by array comparative genomic hybridisationV Malan, O Raoul, H V Firth, et al.
Pageof 23